FDA Inspection 753325 — Kaltron, Inc.

Kaltron, Inc. — FEI 3000126943

The FDA completed an inspection of Kaltron, Inc. on Nov 7, 2011 in Bensenville, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 7, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bensenville, IL (United States)